High-throughput sequencing of the paired human immunoglobulin heavy and light chain repertoire
By B. DeKosky, G. Ippolito, Ryan P Deschner, Jason J. Lavinder, Y. Wine, Brandon M. Rawlings, N. Varadarajan, C. Giesecke, T. Dörner, Sarah F. Andrews and 5 more. 2013
425 citations recorded by the source corpus.
Subfields: Immunology, Radiology, Nuclear Medicine and Imaging
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Immunology
- Jeffrey J. Gray
- Adam J. Riesselman
- Christopher Sander
- Jung-Eun Shin
- Aaron W. Kollasch
- Elana Simon
- A. Manglik
- Debora Marks
In Radiology, Nuclear Medicine and Imaging
- Jeffrey J. Gray
- Daisuke Kuroda
- Adam J. Riesselman
- Christopher Sander
- Jung-Eun Shin
- Aaron W. Kollasch
- Elana Simon
- A. Manglik
Citations in the corpus
- Protein design and variant prediction using autoregressive generative models (2021, background): “Paired antibody chains are more challenging to sequence than nanobodies, but more repertoires are becoming available 91 .”
- Large-scale sequence and structural comparisons of human naive and antigen-experienced antibody repertoires (2016, methodology): “MiSeq 2 × 300 technology permits sequencing 600 bp of the ∼850-bp VH:VL amplicon per sample, and therefore full-length VH and VL genes for AEBCs were generated via bioinformatic assembly of the separate VH, VL, and VH:VL sequencing samples as described previously (29, 30, 33, 34).”